Source: ALL
Variant DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Disease Class Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs12742393
rs12742393
0.925 0.120 1 162254796 intron variant A/C;T snv
Diabetes Mellitus, Non-Insulin-Dependent
Nutritional and Metabolic Diseases; Endocrine System Diseases 0.030 1.000 3 2010 2019
dbSNP: rs12742393
rs12742393
0.925 0.120 1 162254796 intron variant A/C;T snv
CUI: C0036341
Disease: Schizophrenia
Schizophrenia
Mental Disorders 0.020 1.000 2 2009 2018
dbSNP: rs1337068
rs1337068
1 162163356 intron variant G/A snv 0.96
CUI: C0202236
Disease: Triglycerides measurement
Triglycerides measurement
0.700 1.000 1 2012 2012
dbSNP: rs1415259
rs1415259
0.925 0.080 1 162115519 intron variant C/T snv 0.54
QT interval feature (observable entity)
0.700 1.000 2 2010 2019
dbSNP: rs1415259
rs1415259
0.925 0.080 1 162115519 intron variant C/T snv 0.54
CUI: C0011581
Disease: Depressive disorder
Depressive disorder
Mental Disorders 0.010 1.000 1 2015 2015
dbSNP: rs1415259
rs1415259
0.925 0.080 1 162115519 intron variant C/T snv 0.54
CUI: C0011570
Disease: Mental Depression
Mental Depression
Behavior and Behavior Mechanisms 0.010 1.000 1 2015 2015
dbSNP: rs1415259
rs1415259
0.925 0.080 1 162115519 intron variant C/T snv 0.54
CUI: C0344315
Disease: Depressed mood
Depressed mood
Behavior and Behavior Mechanisms 0.010 1.000 1 2015 2015
dbSNP: rs1415259
rs1415259
0.925 0.080 1 162115519 intron variant C/T snv 0.54
CUI: C1623258
Disease: Electrocardiography
Electrocardiography
0.700 1.000 1 2010 2010
dbSNP: rs141560292
rs141560292
1.000 0.040 1 162154408 missense variant G/A snv 1.6E-05 7.7E-05
CUI: C1510586
Disease: Autism Spectrum Disorders
Autism Spectrum Disorders
Mental Disorders 0.010 1.000 1 2010 2010
dbSNP: rs1477437491
rs1477437491
0.925 0.040 1 162367213 missense variant G/A snv 2.8E-05
CUI: C0028768
Disease: Obsessive-Compulsive Disorder
Obsessive-Compulsive Disorder
Mental Disorders 0.010 1.000 1 2010 2010
dbSNP: rs1477437491
rs1477437491
0.925 0.040 1 162367213 missense variant G/A snv 2.8E-05
CUI: C1510586
Disease: Autism Spectrum Disorders
Autism Spectrum Disorders
Mental Disorders 0.010 1.000 1 2010 2010
dbSNP: rs1510291
rs1510291
1 162358271 intron variant C/T snv 3.5E-02
High density lipoprotein measurement
0.700 1.000 1 2012 2012
dbSNP: rs1510291
rs1510291
1 162358271 intron variant C/T snv 3.5E-02
CUI: C0428472
Disease: Serum HDL cholesterol measurement
Serum HDL cholesterol measurement
0.700 1.000 1 2012 2012
dbSNP: rs164147
rs164147
0.882 0.080 1 162368607 3 prime UTR variant A/C snv 0.76
CUI: C0028754
Disease: Obesity
Obesity
Pathological Conditions, Signs and Symptoms; Nutritional and Metabolic Diseases 0.010 1.000 1 2016 2016
dbSNP: rs164147
rs164147
0.882 0.080 1 162368607 3 prime UTR variant A/C snv 0.76
CUI: C0524620
Disease: Metabolic Syndrome X
Metabolic Syndrome X
Nutritional and Metabolic Diseases 0.010 1.000 1 2016 2016
dbSNP: rs164147
rs164147
0.882 0.080 1 162368607 3 prime UTR variant A/C snv 0.76
CUI: C0020456
Disease: Hyperglycemia
Hyperglycemia
Nutritional and Metabolic Diseases 0.010 1.000 1 2016 2016
dbSNP: rs16857031
rs16857031
1 162143120 intron variant C/G snv 0.18
QT interval feature (observable entity)
0.800 1.000 3 2009 2019
dbSNP: rs16857031
rs16857031
1 162143120 intron variant C/G snv 0.18
CUI: C0007222
Disease: Cardiovascular Diseases
Cardiovascular Diseases
Cardiovascular Diseases 0.010 1.000 1 2015 2015
dbSNP: rs16860953
rs16860953
1 162364127 5 prime UTR variant G/A snv 2.1E-02
CUI: C0428474
Disease: Serum LDL cholesterol measurement
Serum LDL cholesterol measurement
0.700 1.000 1 2012 2012
dbSNP: rs16860953
rs16860953
1 162364127 5 prime UTR variant G/A snv 2.1E-02
Low density lipoprotein cholesterol measurement
0.700 1.000 1 2012 2012
dbSNP: rs17457880
rs17457880
1 162198364 intron variant G/A snv 2.0E-02
QT interval feature (observable entity)
0.700 1.000 1 2014 2014
dbSNP: rs17460657
rs17460657
1 162292036 intron variant A/C snv 4.5E-02
QT interval feature (observable entity)
0.700 1.000 1 2014 2014
dbSNP: rs1858232
rs1858232
0.882 0.080 1 162334048 intron variant A/G;T snv
CUI: C0344315
Disease: Depressed mood
Depressed mood
Behavior and Behavior Mechanisms 0.010 1.000 1 2015 2015
dbSNP: rs1858232
rs1858232
0.882 0.080 1 162334048 intron variant A/G;T snv
CUI: C0036341
Disease: Schizophrenia
Schizophrenia
Mental Disorders 0.010 1.000 1 2015 2015
dbSNP: rs1858232
rs1858232
0.882 0.080 1 162334048 intron variant A/G;T snv
CUI: C0011581
Disease: Depressive disorder
Depressive disorder
Mental Disorders 0.010 1.000 1 2015 2015